3-(1,3-benzodioxol-5-yl)-7-[(2E,5E)-7-hydroxy-3,7-dimethylocta-2,5-dienoxy]-6-methoxychromen-4-one

Details

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Internal ID 5e8dc5c6-fffc-4aaf-a18c-9187cb3a3c38
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Isoflav-2-enes > Isoflavones
IUPAC Name 3-(1,3-benzodioxol-5-yl)-7-[(2E,5E)-7-hydroxy-3,7-dimethylocta-2,5-dienoxy]-6-methoxychromen-4-one
SMILES (Canonical) CC(=CCOC1=C(C=C2C(=C1)OC=C(C2=O)C3=CC4=C(C=C3)OCO4)OC)CC=CC(C)(C)O
SMILES (Isomeric) C/C(=C\COC1=C(C=C2C(=C1)OC=C(C2=O)C3=CC4=C(C=C3)OCO4)OC)/C/C=C/C(C)(C)O
InChI InChI=1S/C27H28O7/c1-17(6-5-10-27(2,3)29)9-11-31-25-14-22-19(13-23(25)30-4)26(28)20(15-32-22)18-7-8-21-24(12-18)34-16-33-21/h5,7-10,12-15,29H,6,11,16H2,1-4H3/b10-5+,17-9+
InChI Key BJBINROOJFYWBC-FOHIQKNHSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C27H28O7
Molecular Weight 464.50 g/mol
Exact Mass 464.18350323 g/mol
Topological Polar Surface Area (TPSA) 83.40 Ų
XlogP 4.70
Atomic LogP (AlogP) 5.24
H-Bond Acceptor 7
H-Bond Donor 1
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-(1,3-benzodioxol-5-yl)-7-[(2E,5E)-7-hydroxy-3,7-dimethylocta-2,5-dienoxy]-6-methoxychromen-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9717 97.17%
Caco-2 - 0.6825 68.25%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.7723 77.23%
OATP2B1 inhibitior - 0.8622 86.22%
OATP1B1 inhibitior + 0.8928 89.28%
OATP1B3 inhibitior + 0.9034 90.34%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9934 99.34%
P-glycoprotein inhibitior + 0.8910 89.10%
P-glycoprotein substrate - 0.5576 55.76%
CYP3A4 substrate + 0.6694 66.94%
CYP2C9 substrate - 0.8167 81.67%
CYP2D6 substrate - 0.8076 80.76%
CYP3A4 inhibition + 0.8424 84.24%
CYP2C9 inhibition + 0.6247 62.47%
CYP2C19 inhibition + 0.7544 75.44%
CYP2D6 inhibition - 0.7965 79.65%
CYP1A2 inhibition - 0.6509 65.09%
CYP2C8 inhibition + 0.6610 66.10%
CYP inhibitory promiscuity + 0.8068 80.68%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5117 51.17%
Eye corrosion - 0.9888 98.88%
Eye irritation - 0.9240 92.40%
Skin irritation - 0.7684 76.84%
Skin corrosion - 0.9439 94.39%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8555 85.55%
Micronuclear - 0.5600 56.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.7859 78.59%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.6864 68.64%
Acute Oral Toxicity (c) I 0.5536 55.36%
Estrogen receptor binding + 0.8826 88.26%
Androgen receptor binding + 0.7892 78.92%
Thyroid receptor binding + 0.6334 63.34%
Glucocorticoid receptor binding + 0.8609 86.09%
Aromatase binding + 0.6505 65.05%
PPAR gamma + 0.8169 81.69%
Honey bee toxicity - 0.7777 77.77%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 1.0000 100.00%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 98.77% 96.77%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.24% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.92% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 96.97% 89.00%
CHEMBL240 Q12809 HERG 95.71% 89.76%
CHEMBL1937 Q92769 Histone deacetylase 2 95.51% 94.75%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.98% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.10% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.22% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.19% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.26% 95.56%
CHEMBL5925 P22413 Ectonucleotide pyrophosphatase/phosphodiesterase family member 1 90.08% 92.38%
CHEMBL3401 O75469 Pregnane X receptor 89.75% 94.73%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 89.71% 92.62%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.61% 96.00%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 88.48% 96.09%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 88.13% 95.78%
CHEMBL2535 P11166 Glucose transporter 86.84% 98.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.32% 96.09%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 82.67% 80.78%
CHEMBL5747 Q92793 CREB-binding protein 82.21% 95.12%
CHEMBL2413 P32246 C-C chemokine receptor type 1 81.12% 89.50%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Millettia conraui

Cross-Links

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PubChem 10647822
LOTUS LTS0209911
wikiData Q104936949